
What do you mean by anomeric carbon? I want an answer preferably for anomeric carbon in carbohydrates (sugars).
Answer
436.8k+ views
2 likes
Hint: Anomers are epimers of cyclic monosaccharides or glycosides that differ in their C-1 configuration if they are aldoses, or their C-2 configuration if they are ketoses. Anomeric carbon or anomeric core refers to the anomeric carbon in anomers.
Complete answer:
The carbon derived from the carbonyl carbon (the ketone or aldehyde functional group) of the open-chain form of the carbohydrate molecule is known as the anomeric carbon. The method of converting one anomer to the other is known as anomerization.
The anomeric carbon in the cyclic form of sugar is the carbon that was previously part of the carbonyl group in the straight-chain structure.
C1 becomes a chiral centre when the chain becomes a coil.
The anomeric carbon is C1.
The carbonyl group in D-fructose is at C2.
C2 is the anomeric carbon in this case.
Or
The carbon in a monosaccharide (such as glucose) that rotates is an example of anomeric carbon. The carbon (C) connected to two oxygen (O) atoms joined by single bonds determines the anomeric carbon. This rotation results in the formation of two distinct configurations: and -anomers. Carbohydrates can then switch between the and configurations on their own: mutarotation is a term used to describe a mechanism.
Note:
The electronic effect, which is an interaction of the orbitals of the ring O and the substituent bond, causes anomeric carbon to be reactive. The anomeric centre is critical for carbohydrate reactivity because it is where the ring opens, forming the carbonyl group, which is an important functional group.
Complete answer:
The carbon derived from the carbonyl carbon (the ketone or aldehyde functional group) of the open-chain form of the carbohydrate molecule is known as the anomeric carbon. The method of converting one anomer to the other is known as anomerization.
The anomeric carbon in the cyclic form of sugar is the carbon that was previously part of the carbonyl group in the straight-chain structure.
C1 becomes a chiral centre when the chain becomes a coil.
The anomeric carbon is C1.
The carbonyl group in D-fructose is at C2.
C2 is the anomeric carbon in this case.
Or
The carbon in a monosaccharide (such as glucose) that rotates is an example of anomeric carbon. The carbon (C) connected to two oxygen (O) atoms joined by single bonds determines the anomeric carbon. This rotation results in the formation of two distinct configurations: and -anomers. Carbohydrates can then switch between the and configurations on their own: mutarotation is a term used to describe a mechanism.
Note:
The electronic effect, which is an interaction of the orbitals of the ring O and the substituent bond, causes anomeric carbon to be reactive. The anomeric centre is critical for carbohydrate reactivity because it is where the ring opens, forming the carbonyl group, which is an important functional group.
Latest Vedantu courses for you
Grade 11 Science PCM | CBSE | SCHOOL | English
CBSE (2025-26)
School Full course for CBSE students
₹41,848 per year
Recently Updated Pages
Master Class 11 Physics: Engaging Questions & Answers for Success

Master Class 11 Chemistry: Engaging Questions & Answers for Success

Master Class 11 Biology: Engaging Questions & Answers for Success

Class 11 Question and Answer - Your Ultimate Solutions Guide

Master Class 11 Business Studies: Engaging Questions & Answers for Success

Master Class 11 Computer Science: Engaging Questions & Answers for Success

Trending doubts
Explain why it is said like that Mock drill is use class 11 social science CBSE

Which of the following blood vessels in the circulatory class 11 biology CBSE

Difference Between Prokaryotic Cells and Eukaryotic Cells

1 ton equals to A 100 kg B 1000 kg C 10 kg D 10000 class 11 physics CBSE

One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

Which one is a true fish A Jellyfish B Starfish C Dogfish class 11 biology CBSE
